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A genome guided evaluation of the Lab4 probiotic consortium.
Baker, L M; Webberley, T S; Masetti, G; Hughes, T R; Marchesi, J R; Jack, A A; Joyce, T S C; Allen, M D; Plummer, S F; Michael, D R; Ramanathan, G; Del Sol, R; Facey, P D.
Affiliation
  • Baker LM; Swansea University Medical School, Swansea University, Singleton Park Campus, Swansea SA2 8PP, United Kingdom.
  • Webberley TS; Cultech Limited, Unit 2 Christchurch Road, Baglan Industrial Park, Port Talbot SA12 7BZ, United Kingdom.
  • Masetti G; Cultech Limited, Unit 2 Christchurch Road, Baglan Industrial Park, Port Talbot SA12 7BZ, United Kingdom.
  • Hughes TR; Systems Immunity Research Institute, Henry Welcome Building, Cardiff University, CF14 4XN, United Kingdom.
  • Marchesi JR; Division of Digestive Diseases, Department of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London, United Kingdom.
  • Jack AA; Cultech Limited, Unit 2 Christchurch Road, Baglan Industrial Park, Port Talbot SA12 7BZ, United Kingdom.
  • Joyce TSC; Cultech Limited, Unit 2 Christchurch Road, Baglan Industrial Park, Port Talbot SA12 7BZ, United Kingdom.
  • Allen MD; Cultech Limited, Unit 2 Christchurch Road, Baglan Industrial Park, Port Talbot SA12 7BZ, United Kingdom.
  • Plummer SF; Cultech Limited, Unit 2 Christchurch Road, Baglan Industrial Park, Port Talbot SA12 7BZ, United Kingdom.
  • Michael DR; Cultech Limited, Unit 2 Christchurch Road, Baglan Industrial Park, Port Talbot SA12 7BZ, United Kingdom.
  • Ramanathan G; Pharmacology based Clinical Trials, Pennington Biomedical Research Center, 6400 Perkins Rd, Baton Rouge, LA 70808, USA.
  • Del Sol R; Swansea University Medical School, Swansea University, Singleton Park Campus, Swansea SA2 8PP, United Kingdom.
  • Facey PD; Swansea University Medical School, Swansea University, Singleton Park Campus, Swansea SA2 8PP, United Kingdom. Electronic address: P.Facey@swansea.ac.uk.
Genomics ; 113(6): 4028-4038, 2021 11.
Article in En | MEDLINE | ID: mdl-34391865
ABSTRACT
Draft genome sequences of the Lab4 probiotic consortium were deposited in Genbank Bifidobacterium animalis subsp lactis CUL34 (PRJNA482550), Bifidobacterium bifidum CUL20 (PRJNA559984), Lactobacillus acidophilus CUL60 (PRJNA482335), Lactobacillus acidophilus CUL21 (PRJNA482434). Probiogenomic analyses confirmed existing taxonomies and identified putative gene sequences that were functionally related to the performance of each organism during in vitro assessments of bile and acid tolerability, adherence to enterocytes and susceptibility to antibiotics. Genomic stability predictions identified no significant risk of gene acquisition of both antibiotic resistance and virulence genes. These observations were supported by acute phase and repeat dose tolerability studies in Wistar rats. High doses of Lab4 did not result in mortalities, clinical/histopathological abnormalities nor systemic toxicity. Increased faecal numbers of Lab4 in supplemented rats implied survival through the gastrointestinal tract and/or impact the intestinal microbiota composition. In summary, this study provides multifaceted support for probiotic functionality and the safety of the Lab4 consortium.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bifidobacterium / Probiotics Type of study: Prognostic_studies Limits: Animals Language: En Journal: Genomics Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bifidobacterium / Probiotics Type of study: Prognostic_studies Limits: Animals Language: En Journal: Genomics Year: 2021 Document type: Article